Prophylactic potential of resiquimod against very virulent infectious bursal disease virus (vvIBDV) challenge in the chicken

被引:18
|
作者
Annamalai, Arunsaravanakumar [1 ]
Ramakrishnan, Saravanan [1 ]
Sachan, Swati [1 ]
Kumar, B. S. Anand [1 ]
Sharma, Bal Krishan [1 ]
Kumar, Vimal [1 ]
Palanivelu, Munuswamy [2 ]
Varghese, Berin P. [2 ]
Kumar, Ajay [3 ]
Saravanan, B. C. [4 ]
Krishnaswamy, Narayanan [5 ]
机构
[1] Indian Vet Res Inst, Immunol Sect, Bareilly 243122, Uttar Pradesh, India
[2] Indian Vet Res Inst, Div Pathol, Bareilly 243122, Uttar Pradesh, India
[3] Indian Vet Res Inst, Div Anim Biochem, Bareilly 243122, Uttar Pradesh, India
[4] Indian Vet Res Inst, Div Parasitol, Bareilly 243122, Uttar Pradesh, India
[5] Indian Vet Res Inst, Div Anim Reprod, Bareilly 243122, Uttar Pradesh, India
关键词
Toll-like receptors; Prophylaxis; Real time PCR; Infectious bursal disease; Resiquimod; Immune response genes; Chicken; BLOOD MONONUCLEAR-CELLS; DOUBLE-STRANDED-RNA; NITRIC-OXIDE; IN-VITRO; CYTOKINE PRODUCTION; SIGNALING PATHWAY; TH2; RESPONSE; TOLL; TLR7; INTERFERON;
D O I
10.1016/j.vetmic.2016.03.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The study evaluated the prophylactic potential of resiquimod (R-848), a synthetic TLR7 agonist, against very virulent infectious bursal disease virus (vvIBDV) infection in chicken. Specific pathogen free White Leghorn chicks of three week age were treated with R-848 (50 mu g/bird, intramuscular) or PBS (n = 26/group). Twenty four hour later, half of the birds from each group were challenged with 10(5) ELD50 of vvIBDV and observed for 10 days. To understand the effect of R-848, immune response genes such as interferon (IFN)-beta, IFN-gamma, IL-1 beta, IL-4, iNOS and TLR7 were analyzed at 24 and 48 h post-challenge in PBMCs ex vivo by real-time PCR (n = 6/group). On day 4 post-challenge, representative birds (n=3/group) were sacrificed to study the bursal damage and IBDV antigen clearance. Immunosuppression was assessed by antibody response against live Newcastle disease virus (NDV) vaccine, which was administered on day 10 post-challenge. R-848 pre-treatment significantly upregulated the transcripts of each immune response gene studied (P < 0.05). There was 50% mortality on vvIBDV challenge in control birds, while it was only 20% with R-848 group. R-848 pre-treatment reduced the bursal damage as indicated by lower bursal lesion score in histopathology, reduced IBDV antigen signal in immunohistochemistry and improved antigen clearance in agar gel immunodiffusion test. Further, it protected significantly against vvIBDV induced immunosuppression as indicated by HI antibody titre. It is concluded that pre-treatment of R-848 conferred partial protection from mortality and bursal damage while complete protection against immunosuppression in chicken when challenged with vvIBDV, which could be due to the upregulation of immune response genes. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 30
页数:10
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